ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.375C>G (p.Leu125=)

dbSNP: rs2541951365
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003045131 SCV003351426 likely benign Fanconi anemia 2022-05-06 criteria provided, single submitter clinical testing

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